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Journal Abstract Search

139 related items for PubMed ID: 18988861

  • 1. Quebec platelet disorder is linked to the urokinase plasminogen activator gene (PLAU) and increases expression of the linked allele in megakaryocytes.
    Diamandis M, Paterson AD, Rommens JM, Veljkovic DK, Blavignac J, Bulman DE, Waye JS, Derome F, Rivard GE, Hayward CP.
    Blood; 2009 Feb 12; 113(7):1543-6. PubMed ID: 18988861
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  • 9. Quebec platelet disorder: features, pathogenesis and treatment.
    Diamandis M, Veljkovic DK, Maurer-Spurej E, Rivard GE, Hayward CP.
    Blood Coagul Fibrinolysis; 2008 Mar 12; 19(2):109-19. PubMed ID: 18277131
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  • 10. Intracellular activation of the fibrinolytic cascade in the Quebec Platelet Disorder.
    Sheth PM, Kahr WH, Haq MA, Veljkovic DK, Rivard GE, Hayward CP.
    Thromb Haemost; 2003 Aug 12; 90(2):293-8. PubMed ID: 12888877
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  • 11. Thrombin generation abnormalities in Quebec platelet disorder.
    Brunet JG, Sharma T, Tasneem S, Liang M, Wilson MD, Rivard GE, Hayward CPM.
    Int J Lab Hematol; 2020 Dec 12; 42(6):801-809. PubMed ID: 32761872
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  • 13. Elevated amyloid beta protein (Abeta42) and late onset Alzheimer's disease are associated with single nucleotide polymorphisms in the urokinase-type plasminogen activator gene.
    Ertekin-Taner N, Ronald J, Feuk L, Prince J, Tucker M, Younkin L, Hella M, Jain S, Hackett A, Scanlin L, Kelly J, Kihiko-Ehman M, Neltner M, Hersh L, Kindy M, Markesbery W, Hutton M, de Andrade M, Petersen RC, Graff-Radford N, Estus S, Brookes AJ, Younkin SG.
    Hum Mol Genet; 2005 Feb 01; 14(3):447-60. PubMed ID: 15615772
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  • 14. Association of late-onset Alzheimer disease with a genotype of PLAU, the gene encoding urokinase-type plasminogen activator on chromosome 10q22.2.
    Finckh U, van Hadeln K, Müller-Thomsen T, Alberici A, Binetti G, Hock C, Nitsch RM, Stoppe G, Reiss J, Gal A.
    Neurogenetics; 2003 Aug 01; 4(4):213-7. PubMed ID: 12898287
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  • 15. Association of urokinase-type plasminogen activator with asthma and atopy.
    Bégin P, Tremblay K, Daley D, Lemire M, Claveau S, Salesse C, Kacel S, Montpetit A, Becker A, Chan-Yeung M, Kozyrskyj AL, Hudson TJ, Laprise C.
    Am J Respir Crit Care Med; 2007 Jun 01; 175(11):1109-16. PubMed ID: 17363771
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  • 16. Bleeding risks associated with inheritance of the Quebec platelet disorder.
    McKay H, Derome F, Haq MA, Whittaker S, Arnold E, Adam F, Heddle NM, Rivard GE, Hayward CP.
    Blood; 2004 Jul 01; 104(1):159-65. PubMed ID: 15026313
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  • 17. Inherited disorders of the fibrinolytic pathway.
    Jain S, Acharya SS.
    Transfus Apher Sci; 2019 Oct 01; 58(5):572-577. PubMed ID: 31427261
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  • 18. Evaluation of urokinase plasminogen activator in urine from individuals with Quebec platelet disorder.
    Diamandis M, Veljkovic DK, Derome F, Rivard GE, Hayward CP.
    Blood Coagul Fibrinolysis; 2008 Jul 01; 19(5):463-4. PubMed ID: 18600101
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  • 19. Association between urokinase-plasminogen activator gene T4065C polymorphism and risk of mitral valve prolapse.
    Chou HT, Chen YT, Wu JY, Tsai FJ.
    Int J Cardiol; 2004 Aug 01; 96(2):165-70. PubMed ID: 15262029
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  • 20. The human urokinase-plasminogen activator gene (PLAU) is located on chromosome 10q24 centromeric to the HOX11 gene.
    Stein PM, Stass SA, Kagan J.
    Genomics; 1993 Apr 01; 16(1):301-2. PubMed ID: 8098010
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